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P268S in NOD2 associates with susceptibility to Parkinson’s disease in Chinese population
BACKGROUND: The cause of almost all cases of Parkinson’s disease (PD) remains unknown. Recent years have seen an explosion in the rate of discovery of genetic defects linked to PD. Different racial and geographical populations may have different distributions of genetic variants. METHODS: In the cur...
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| Glavni autori: | , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2013
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3662627/ https://ncbi.nlm.nih.gov/pubmed/23651603 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-9081-9-19 |
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